Skip navigation
Please use this identifier to cite or link to this item: http://uvadoc.uva.es/handle/10324/21453
Title: Prolinamides as Asymmetric Organocatalysts
Authors: Pedrosa Sáez, Rafael
Andrés García, José María
Issue Date: 2015
Publisher: Royal Society of Chemistry
Description: Producción Científica
Citation: Sustainable Catalysis: Without Metals or Other Endangered Elements, Part 1. Editor, Michael North. 2015, Chapter 6, p.120-139
Abstract: Prolinamides are valuable organocatalysts for enantioselective transformations that occur by activation of the nucleophile by enamine formation. Different substituents can be appended on the nitrogen atom of the carboxamide, which allow for the modulation of the catalytic properties. In that way, the acidity, the hydrogen donor properties, the hydrophobicity, or the chiral environment can be modified, in a few steps, starting from easily available proline.
Keywords: Química orgánica
ISBN: 978-1-78262-209-3
Sponsor: Ministerio de Economía, Industria y Competitividad (CTQ2014-59870-P)
Junta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA064U13)
Publisher Version: http://pubs.rsc.org/
Rights Owner: © The Royal Society of Chemistry
Language: eng
URI: http://uvadoc.uva.es/handle/10324/21453
Rights: info:eu-repo/semantics/restrictedAccess
Appears in Collections:DEP67 - Capítulos de monografías

Files in This Item:
File Description SizeFormat 
Chapter-6-Abstract-Susutainable-Catalysis.pdf27,71 kBAdobe PDFThumbnail
View/Open

This item is licensed under a Creative Commons License Creative Commons

Suggestions
University of Valladolid
Powered by MIT's. DSpace software, Version 5.5
UVa-STIC